A Prospective Cohort Study of Exercise Rehabilitation in the Treatment of Parkinson's Disease

Sponsor
Ruijin Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT05447975
Collaborator
(none)
394
2
72

Study Details

Study Description

Brief Summary

The investigators proposed to conduct a cohort study to observe whether Tai Chi intervention could delay the disease progression of Parkinson's disease (PD).

PD patients were enrolled into 5 Tai Chi classes which began at different timepoints from Jan. 2016 to Jan. 2019. Each participant was assessed before participants joined the Tai Chi class. After the recruitment, participants accepted continuous Tai Chi training in the classes till the last follow-up. The investigators performed three times of follow-up in Nov.

  • Dec. 2019, Oct. - Nov. 2020 and Jun. - July 2021. Using propensity score matching, the investigators matched PD patients who did not receive Tai Chi training as control group in gender, disease duration, age, and Hoehn - Yahr staging. The aim is to observe the effect of Tai Chi on delaying the disease progression of PD.
Condition or Disease Intervention/Treatment Phase
  • Other: Tai Chi training
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
394 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
A Prospective Cohort Study of Exercise Rehabilitation in the Treatment of Parkinson's Disease
Actual Study Start Date :
Jan 1, 2016
Actual Primary Completion Date :
Jul 31, 2021
Actual Study Completion Date :
Jan 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Tai Chi group

Other: Tai Chi training
As for Tai Chi training, standardized Tai Chi was taught by professional Tai Chi coaches from Sino Taiji of Fuxing International in classes: Qishi ("Starting Posture"), Shangsanbu ("Twist Step"), Yema Fenzong("Part the Wild Horse's Mane on Both Side"), Jingang Daozhui ("Buddha's warrior attendant pounds mortar"), Shoushi ("Closing Posture"). Patients participated in this class were trained, twice a week, 60 min per time. PD patients whose attendance rate less than 75% were excluded.

No Intervention: Control

Outcome Measures

Primary Outcome Measures

  1. the annual change of UPDRS total score measured in "ON" state at three follow-ups [1 year]

    the annual change of Unified Parkinson's Disease Rating Scale (UPDRS) total score measured in "ON" state at three follow-ups. The range of UPDRS is between 0 and 207. The higher score means a worse outcome.

Eligibility Criteria

Criteria

Ages Eligible for Study:
50 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Clinical diagnosis of Parkinson's disease according to 2015 MDS diagnostic criteria and United Kingdom Brain Bank diagnostic criteria in 1992;

  2. Hoehn - Yahr staging: 1 - 2.5;

  3. The medication was stable at least 3 months before recruiting and not changed during follow-up unless increasing antiparkinsonian drugs or the need of deep brain stimulation (DBS) is required according to the disease severity;

Exclusion Criteria:
  1. Secondary causes, such as inflammatory, drug-induced, vascular and toxin-induced parkinsonism.

  2. Parkinsonism with other neurodegenerative diseases, such as progressive supranuclear palsy, multiple system atrophy, cortical basal ganglia degeneration, Wilson's disease.

  3. Other neurological diseases, such as stroke.

  4. Patients who were receiving any other clinical trials or regular exercise protocols.

  5. Patients who had fall incidents in the 6 months before recruiting due to safety considerations.

  6. Patients whose Mini-Mental State Examination (MMSE) scores were less than 24.

  7. Patients who had medical history that did not fit to exercise, such as orthopedics diseases or cardiopulmonary dysfunction.

  8. Patients who received education less than 6 years.

  9. Patients who could not walk and live independently.

  10. Patients who received brain surgery (e.g. deep brain stimulation);

  11. Patients whose exercise length longer than 50 minutes per week.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Ruijin Hospital

Investigators

None specified.

Study Documents (Full-Text)

More Information

Publications

None provided.
Responsible Party:
Shengdi Chen, Professor, Ruijin Hospital
ClinicalTrials.gov Identifier:
NCT05447975
Other Study ID Numbers:
  • RuijinH-202205
First Posted:
Jul 7, 2022
Last Update Posted:
Jul 7, 2022
Last Verified:
Jul 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 7, 2022